US2022340910A1PendingUtilityA1
Sugar chain-related gene and use thereof
Est. expiryDec 27, 2027(~1.4 yrs left)· nominal 20-yr term from priority
G01N 2333/91194C12N 2310/14A61P 1/16A61P 25/28A61K 31/7105A61K 38/43G01N 33/5023C12N 9/13C12Q 1/485A61P 29/00A61P 19/02A61P 9/10C12N 15/1137A61P 9/04C12Q 1/48A61P 27/02A61P 13/10A61P 1/04A61P 3/10A61P 25/18A61P 31/14Y10T436/143333A61P 21/00A61P 25/00A61P 9/00A61P 19/04A61P 7/00A61P 21/04A61P 3/00A61P 37/08A61P 7/02A61P 31/20A61P 15/10A61P 1/00A61P 13/12A61P 1/18A61P 11/00A61P 17/00A61P 25/16A61P 25/02A61P 37/02A61P 43/00A61P 13/08A61P 9/06
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Claims
Abstract
As a result of dedicated studies, the present inventors succeeded in discovering, for the first time, that fibrogenesis could be suppressed at the physiological tissue level by inhibiting sulfation at position 4 or 6 of GalNAc, which is a sugar that constitutes sugar chains. Furthermore, the present inventors conducted studies using various disease model animals, and as a result, successfully demonstrated that inhibitors of sulfation at position 4 or 6 of GalNAc had therapeutic effects on diseases caused by tissue fibrogenesis (tissue fibrogenic disorders).
Claims
exact text as granted — not AI-modified1 . A tissue fibrogenesis suppressing-agent, comprising:
an inhibitor of sulfation at position 4 or 6 of N-acetylgalactosamine, wherein the inhibitor is an siRNA that suppresses expression of the GalNAc4S-6ST gene.
2 .- 12 (canceled)
13 . A method of treating a fibrogenic disorder, comprising:
identifying a subject having a fibrogenic disorder of a tissue selected from the group consisting of cardiac tissue, gastrointestinal tissue, lung tissue, pancreatic tissue, kidney tissue, ocular tissue, cranial nerve tissue, and skin tissue; and administering to the subject a therapeutically effective amount of an siRNA that suppresses expression of a gene encoding a sulfotransferase that transfers a sulfate to position 4 or 6 of N-acetylgalactosamine; wherein the siRNA suppresses expression of a nucleotide sequence selected from the group consisting of a GalNAc4S-6ST gene, a GalNAc4ST-1 gene, a GalNAc4ST-2 gene, a C4ST-1 gene, a C4ST-2 gene, a C4ST-3 gene, a C6ST-1 gene, a C6ST-2 gene, and a D4ST gene.
14 . The method of claim 13 , wherein the subject has a fibrogenic disorder of gastrointestinal tissues.
15 . The method of claim 14 , wherein the siRNA suppresses expression of the GalNAc4S-6ST gene.
16 . The method of claim 13 , wherein the gene encoding a sulfotransferase is a human gene.
17 . The tissue fibrogenesis suppressing-agent of claim 1 , wherein the inhibitor is siRNA comprising the sequences of SEQ ID NO: 25 and SEQ ID NO: 26.
18 . The tissue fibrogenesis suppressing-agent of claim 1 , comprising:
the inhibitor; and a pharmaceutically acceptable carrier.
19 . The tissue fibrogenesis suppressing-agent of claim 17 , comprising:
the inhibitor; and a pharmaceutically acceptable carrier.
20 . A siRNA comprising the sequences of SEQ ID NO: 25 and SEQ ID NO: 26.
21 . A composition, comprising:
the siRNA of claim 20 ; and a pharmaceutically acceptable carrier.
22 . A composition, comprising:
the siRNA of claim 20 ; and a pharmaceutically acceptable carrier, wherein the composition has a therapeutic effect on a tissue fibrogenic disorder.
23 . A composition, comprising:
the siRNA of claim 20 ; and a pharmaceutically acceptable carrier, wherein the composition has a therapeutic effect on an inflammatory bowel disease.
24 . A composition, comprising:
the siRNA of claim 20 ; and a pharmaceutically acceptable carrier, wherein the composition has a therapeutic effect on Crohn's disease.
25 . A composition, comprising:
the siRNA of claim 20 ; and a pharmaceutically acceptable carrier, wherein the composition has a therapeutic effect on ulcerative colitis.Join the waitlist — get patent alerts
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